37535-87-8

Usage

Properties

1. Molecular formula: C12H17NS
2. Physical form: yellow to light brown crystalline solid
3. Trade names: Santoflex, Flexzone, Naugard Cure One
4. Function: antioxidant, antiozonant, stabilizer, corrosion inhibitor
5. Applications: rubber compounds, polymers, hair dyes, oilfield chemicals

Specific content

Used as an intermediate in the synthesis of dyes and pharmaceuticals
Functions as an antioxidant and antiozonant in rubber compounds to prevent aging and cracking
Acts as a stabilizer in the production of polymers
Found in some hair dyes and coloring products
Functions as a corrosion inhibitor in various industrial applications
Employed in the manufacturing of oilfield chemicals

Upstream product

• 7439-89-6 iron 
• 76706-88-2 Cyclohexyl-(2-nitrophenyl)-sulfid 
• 1569-69-3 Cyclohexanethiol 
• 615-43-0 2-iodophenylamine 
• 626-62-0 Cyclohexyl iodide 
• 137-07-5 2-amino-benzenethiol 

Downstream Products

• 40115-03-5 2-cyclohexyl-benzothiazole 
• 720675-16-1 bbenzo[d]thiazol-2-yldiphenylphosphine oxide 

Relevant academic research and scientific papers

Di- tert-butyl Peroxide-Mediated Radical C(sp2/sp3)-S Bond Cleavage and Group-Transfer Cyclization

A novel strategy of cascade radical C(sp2/sp3)-S bond cleavage and group-transfer cyclization is disclosed. Triggered by alkyl radicals, varieties of 2-isocyanoaryl thioethers containing aliphatic, aryl, and heteroaromatic groups can be cleaved and precisely reinstalled to give benzothiazole derivatives. Mechanistic studies reveal that the cascade reaction undertakes an intermolecular pathway, and the inner radical sources (R radicals) exhibit high priority over those of methyl radical origin from di-tert-butyl peroxide.

An efficient copper-catalyzed cross-coupling reaction of thiols with aryl iodides

Commercially available Cu2O powder is a very reactive catalyst for the coupling of thiols to aryl iodides. A variety of functional groups including esters, unprotected amines, alcohols, and heterocycles tolerate the reaction conditions. Moreover, di-ortho-substituted aryl iodides with sterically demanding substrates were also coupled to give the desired aryl thioethers in good to excellent yields. Copyright

Sulfonanilide compounds

Sulfonanilide compounds represented by the formula STR1 wherein R1 is a lower alkyl group or a trifluoromethyl group, R2 is a cycloalkylidenemethyl group, a group of the formula --A--R3 (wherein A is an oxygen atom, a sulf